6 дней назад
Senior Clinical Research Associate (Clinical Monitoring)
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Clinical Research Associate (Clinical Monitoring): Conducting countrywide clinical trial monitoring across remote and onsite settings with an accent on data integrity, patient safety, regulatory compliance, and Trial Master File management. Focus on planning and executing qualification, initiation, interim, and close-out visits, reviewing essential site documents, and monitoring studies across cardiovascular, oncology, rare disease, and CNS therapeutic areas.
Location: Portugal; fully home based with countrywide monitoring, including an average of 6 monitoring days per month at hospital sites in Lisbon, Porto, and Coimbra.
Contract/freelance full-time engagement for up to 1 year.
Company
Clinical research services supporting biotech, medtech, and specialty pharma organizations in developing medicines, medical devices, and diagnostics.
What you will do
- Conduct countrywide clinical trial monitoring through remote, onsite, or other approved methods.
- Prepare for and conduct site qualification, study initiation, interim monitoring, and close-out visits.
- Plan daily monitoring activities and set priorities for investigator sites.
- Deliver timely, high-quality monitoring reports for sponsor approval.
- Maintain the Trial Master File and electronic Trial Master File according to filing guidelines.
- Review site documents for accuracy, completeness, currency, and compliance with ICH/GCP essential document requirements.
Requirements
- Degree or equivalent experience in a clinical, scientific, or health-related field, or qualification as a licensed healthcare professional.
- Previous clinical research experience and completion of a CRA training program.
- At least 4 years of independent monitoring experience.
- Experience across therapeutic areas such as cardiovascular disease, oncology, rare diseases, or CNS conditions including Alzheimer’s and Parkinson’s disease.
- Availability for countrywide monitoring in Portugal, including an average of 6 monitoring days per month.
- Spanish proficiency is highly desirable for potential monitoring activities in Spain.
Culture & Benefits
- Fully home based working arrangement.
- Full-time contract/freelance engagement lasting up to 1 year.
- Flexible working practices designed to support work-life balance and professional growth.
- Opportunity to contribute to clinical research supporting new medicines, devices, and diagnostics.
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